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Classification, diagnosis and potential mechanisms in Pontocerebellar Hypoplasia
Pontocerebellar Hypoplasia (PCH) is group of very rare, inherited progressive neurodegenerative disorders with prenatal onset. Up to now seven different subtypes have been reported (PCH1-7). The incidence of each subtype is unknown. All subtypes share common characteristics, including hypoplasia/atr...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3159098/ https://ncbi.nlm.nih.gov/pubmed/21749694 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1750-1172-6-50 |
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